You are here

IDE Submissions Workshop – Fall 2019

October 9, 2019
Washington, DC
Regulatory
Workshop

Click here to view the agenda

During this interactive workshop, FDA and industry experts will lead you through the regulatory and practical guidelines governing when an investigational device exemption (IDE) is required.

Agenda topics include:

  • The purpose of an IDE
  • Tips on making the best use of pre-submission meetings
  • Components of a successful IDE submission
  • Common errors and deficiencies in an IDE application
  • The ins and outs of BIMO inspections
  • Details about the regulatory requirements needed during trial conduct
  • And more!

The IDE Submissions Workshop will take place October 9 at the AdvaMed Office in Washington, DC.

View hotel list

Address:
701 Pennsylvania Ave. N.W.
Suite 800
Washington, D.C.

Registration Fees

AdvaMed Member Registration: $1,595.00

Accel Member Registration: $695.00

Government and Non-Profit Registration: $695.00

Non-Member Registration: $2,095.00

Note: Early-bird pricing is available for AdvaMed Members and Non-Members. Register by September 6, 2019 for $200 off your registration! Also, check your confirmation email for opportunities to save even more on your next workshop!

Please review our cancellation policy here